UMR7039 CRAN, Institut de Cancérologie de Lorraine, CNRS, Université de Lorraine, 6 Avenue de Bourgogne, 54519, Vandoeuvre-lès-Nancy, France.
UMR 7365 CNRS-UL, IMoPA, Vandœuvre-lès-Nancy, France.
Sci Rep. 2020 Dec 4;10(1):21273. doi: 10.1038/s41598-020-78087-7.
Radiation-induced fibrosis (RIF) is the main late radiation toxicity in breast cancer patients. Most of the current 3D in vitro breast cancer models are composed by cancer cells only and are unable to reproduce the complex cellular homeostasis within the tumor microenvironment to study RIF mechanisms. In order to account complex cellular interactions within the tumor microenvironment, an advanced 3D spheroid model, consisting of the luminal breast cancer MCF-7 cells and MRC-5 fibroblasts, was developed. The spheroids were generated using the liquid overlay technique in culture media into 96-well plates previously coated with 1% agarose (m/v, in water). In total, 21 experimental setups were tested during the optimization of the model. The generated spheroids were characterized using fluorescence imaging, immunohistology and immunohistochemistry. The expression of ECM components was confirmed in co-culture spheroids. Using α-SMA staining, we confirmed the differentiation of healthy fibroblasts into myofibroblasts upon the co-culturing with cancer cells. The induction of fibrosis was studied in spheroids treated 24 h with 10 ng/mL TGF-β and/or 2 Gy irradiation. Overall, the developed advanced 3D stroma-rich in vitro model of breast cancer provides a possibility to study fibrosis mechanisms taking into account 3D arrangement of the complex tumor microenvironment.
辐射诱导纤维化(RIF)是乳腺癌患者的主要晚期放射毒性。目前大多数的 3D 体外乳腺癌模型仅由癌细胞组成,无法复制肿瘤微环境中的复杂细胞内稳态,从而无法研究 RIF 机制。为了研究肿瘤微环境中的复杂细胞相互作用,开发了一种先进的 3D 球体模型,该模型由腔乳腺癌 MCF-7 细胞和 MRC-5 成纤维细胞组成。使用液体覆盖技术在先前用 1%琼脂糖(m/v,在水中)涂覆的 96 孔板中的培养基中生成球体。在模型优化过程中总共测试了 21 个实验设置。使用荧光成像、免疫组织化学和免疫组织化学对生成的球体进行了表征。在共培养球体中证实了细胞外基质成分的表达。使用 α-SMA 染色,我们证实了在与癌细胞共培养时健康成纤维细胞分化为肌成纤维细胞。研究了用 10ng/mL TGF-β和/或 2Gy 照射处理 24 小时后的球体中的纤维化诱导。总之,开发的富含基质的先进 3D 乳腺癌体外模型提供了一种可能性,可以研究考虑到复杂肿瘤微环境的 3D 排列的纤维化机制。